Canonical Allele Identifier: CA1467599773
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313664A= , CM000666.2:g.72313664A= GRCh38
NC_000004.11:g.73179381A= , CM000666.1:g.73179381A= GRCh37
NC_000004.10:g.73398245A= NCBI36
NG_046955.1:g.260136T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1745+13T= MANE Select ENSP00000286657.4:n.1745+13T=
ENST00000286657.8:c.1745+13T= ENSP00000286657.4:n.1745+13T=
ENST00000622135.1:c.1745+13T= ENSP00000480055.1:n.1745+13T=
NM_014243.2:c.1745+13T= NP_055058.2:n.1745+13T=
XM_011532421.1:c.1688+13T= XP_011530723.1:n.1688+13T=
XM_011532422.1:c.1661+13T= XP_011530724.1:n.1661+13T=
XM_011532423.1:c.1103+13T= XP_011530725.1:n.1103+13T=
XM_011532424.1:c.1013+13T= XP_011530726.1:n.1013+13T=
XM_011532421.2:c.1688+13T= XP_011530723.1:n.1688+13T=
XM_011532422.3:c.1661+13T= XP_011530724.1:n.1661+13T=
NM_014243.3:c.1745+13T= MANE Select NP_055058.2:n.1745+13T=